Canonical Allele Identifier: CA2565410869

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.195007044T>C , CM000664.2:g.195007044T>C	GRCh38
NC_000002.11:g.195871768T>C , CM000664.1:g.195871768T>C	GRCh37
NC_000002.10:g.195580013T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_001739836.1:n.553+52391A>G